Pelvalon, Inc. is one of 4902 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pelvalon, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Pelvalon, Inc. has 1 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Pelvalon, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pelvalon, Inc.
1 devices